Development of a comprehensive noninvasive prenatal test (2018)
- Authors:
- USP affiliated authors: LOURENÇO, NAILA CRISTINA VILAÇA - IB ; LOPES, MARCO ANTONIO BORGES - FM ; ZATZ, MAYANA - IB ; BERTOLA, DÉBORA ROMEO - IB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB
- Unidades: IB; FM
- DOI: 10.1590/1678-4685-gmb-2017-0177
- Subjects: DIAGNÓSTICO PRÉ-NATAL; SEQUENCIAMENTO GENÉTICO; ANORMALIDADES CROMOSSÔMICAS; GENÉTICA MÉDICA
- Keywords: Cell-free DNA; Next-generation sequencing; Trisomy; Noninvasive prenatal test; Fetal fraction
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher place: Ribeirao Preto
- Date published: 2018
- Source:
- Título: Genetics and Molecular Biology
- ISSN: 1415-4757
- Volume/Número/Paginação/Ano: v. 41, n. 3, p. 545-554, 2018
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
MALCHER, Carolina et al. Development of a comprehensive noninvasive prenatal test. Genetics and Molecular Biology, v. 41, n. 3, p. 545-554, 2018Tradução . . Disponível em: https://doi.org/10.1590/1678-4685-gmb-2017-0177. Acesso em: 28 jan. 2026. -
APA
Malcher, C., Yamamoto, G. L., Burnham, P., Ezquina, S. A. M., Lourenço, N. C. V., Balkassmi, S., et al. (2018). Development of a comprehensive noninvasive prenatal test. Genetics and Molecular Biology, 41( 3), 545-554. doi:10.1590/1678-4685-gmb-2017-0177 -
NLM
Malcher C, Yamamoto GL, Burnham P, Ezquina SAM, Lourenço NCV, Balkassmi S, Antonio DSM, Hsia GSP, Gollop T, Pavanello RC, Lopes MA, Bakker E, Zatz M, Bertola D, Vlaminck ID, Passos-Bueno MR. Development of a comprehensive noninvasive prenatal test [Internet]. Genetics and Molecular Biology. 2018 ; 41( 3): 545-554.[citado 2026 jan. 28 ] Available from: https://doi.org/10.1590/1678-4685-gmb-2017-0177 -
Vancouver
Malcher C, Yamamoto GL, Burnham P, Ezquina SAM, Lourenço NCV, Balkassmi S, Antonio DSM, Hsia GSP, Gollop T, Pavanello RC, Lopes MA, Bakker E, Zatz M, Bertola D, Vlaminck ID, Passos-Bueno MR. Development of a comprehensive noninvasive prenatal test [Internet]. Genetics and Molecular Biology. 2018 ; 41( 3): 545-554.[citado 2026 jan. 28 ] Available from: https://doi.org/10.1590/1678-4685-gmb-2017-0177 - Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice
- Obesity in pycnodysostosis due to UPD1: possible effect of an imprinted gene on chromosome 1
- Challenges in the orthodontic treatment of a patient with pycnodysostosis
- Craniosynostosis in pycnodysostosis: broadening the spectrum of the cranial flat bone abnormalities
- Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries
- A complex chromosomal rearrangement involving chromosomes 2, 5, and X in autism spectrum disorder
- Complexity of the 5′ Untranslated Region of EIF4A3, a Critical Factor for Craniofacial and Neural Development
- Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH)
- Craniosynostosis in 10q26 deletion patients: a consequence of brain underdevelopment or altered suture biology?
- High proportion of new mutations and possible anticipation in brazilian facioscapulohumeral muscular dystrophy families
Informações sobre o DOI: 10.1590/1678-4685-gmb-2017-0177 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
